Evidence map›Paper›PMID 32306195›Full record

ReviewHuman cell2020

The spatiotemporal control of human matriptase action on its physiological substrates: a case against a direct role for matriptase proteolytic activity in profilaggrin processing and desquamation.

Chen-Yong Lin, Jehng-Kang Wang, Michael D Johnson

Abstract readReview
PubMed Publisher
In one paragraph

Review in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Chen-Yong LinDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University School of Medicine, W412 Research Building 3970 Reservoir Road NW, Washington, DC, 20057, USA. lincy@georgetown.edu.ORCID http://orcid.org/0000-0002-6391-2571
Jehng-Kang WangDepartment of Biochemistry National Defense Medical Center, Taipei, 11490, Taiwan.
Michael D JohnsonDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University School of Medicine, W412 Research Building 3970 Reservoir Road NW, Washington, DC, 20057, USA.
Georgetown University · USNational Defense Medical Center · TW

Funding

Mechanisms of Deregulation of Matriptase in Breast CancerR01CA123223 · NCI · GEORGETOWN UNIVERSITY · PI JOHNSON, MICHAEL D, LIN, CHEN-YONG · 2010 to 2014
$1.6M
Chi Mei Medical Center CMNDMC10705Chi Mei Medical Center CMNDMC10813Ministry of National Defense Medical Affair Bureau, Taiwan MAB-108-079NCI NIH HHS CA 123223
6 · The paper itself

Abstract

Studies of human genetic disorders and animal models indicate that matriptase plays essential roles in proteolytic processes associated with profilaggrin processing and desquamation at late stages of epidermal differentiation. The tissue distribution profile and zymogen activation status in human skin, however, suggests that matriptase physiological function in the skin more likely lies in the proliferating and differentiating keratinocytes in the basal and spinous layers. Marked acanthosis with expanded spinous layer and lack of significant changes in intensity and expression pattern for several terminal differentiation markers in the skin of ARIH patients support matriptase's role in earlier rather than the later stages of differentiation. In addition to the tissue distribution, differential subcellular localization further limits the ability of extracellular matriptase proteolytic activity to access the cytosolic non-membrane-bound keratohyalin granules, in which profilaggrin processing occurs. The short lifespan of active matriptase, which results from tightly controlled zymogen activation, rapid inhibition by HAI-1, and shedding from cell surface, indicates that active matriptase likely performs physiological functions via limited proteolysis on its substrates, as needed, rather than via a continuous bulk process. We, here, review these spatiotemporal controls of matriptase proteolytic activity at the biochemical, cellular, and tissue level. Based on this in-depth understanding of how matriptase activity is regulated, we argue that there is no direct involvement of matriptase proteolytic activity in profilaggrin processing and desquamation. The defects in epidermal terminal differentiation associated with matriptase deficiency are likely secondary and are due to putative disruption at earlier stages of differentiation.

Indexed as

ProteolysisAnimalsCell DifferentiationCell ProliferationEnzyme PrecursorsEpidermal CellsFilaggrin ProteinsHumansIntermediate Filament ProteinsKeratinocytesMiceMutationSerine EndopeptidasesEnzyme PrecursorsFilaggrin ProteinsIntermediate Filament ProteinsmatriptaseSerine EndopeptidasesDesquamationMatriptaseProfilaggrin processingProteolytic activityRegulationSkin

Identifiers

PMID32306195
OpenAlexW3017035288

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.